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Cryopreservation of rat islets of Langerhans by vitrification

机译:通过玻璃化冷冻保存郎格罕氏大鼠胰岛

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摘要

Cryopreservation could be a possible means of addressing the shortage of islets of Langerhans. We investigated the effects of EDT324 solution on the vitrification of isolated rat islets of Langerhans. Rat pancreatic islets were cryopreserved in 10% DMSO by a slow-rate freezing method or were cryopreserved in EDT324 solution by vitrification. The cryopreserved islets were compared in terms of viability, stimulation index and metabolic function after transplantation. After cryopreservation, the viability and stimulation of islets stored in EDT324 were 92.4% and 6.4, respectively, and were higher than islets stored by slow freezing (72.5% and 1.5, respectively). Streptozotocininduced diabetic rats were transplanted with islets cryopreserved in EDT324, which corrected diabetes and achieved euglycemia within 2 days after transplantation. These results indicate that EDT324 allows successful cryopreservation of rat islets for long-term storage as an alternative solution to traditionally used solutions, such as 10% DMSO. Transplantation of cryopreserved islets into diabetic rats can achieve euglycemia.
机译:冷冻保存可能是解决朗格罕岛胰岛短缺的一种可能方法。我们研究了EDT324溶液对朗格罕氏分离大鼠胰岛玻璃化的影响。通过慢速冷冻方法将大鼠胰岛冷冻保存在10%DMSO中,或通过玻璃化冷冻保存在EDT324溶液中。比较冷冻保存的胰岛在移植后的活力,刺激指数和代谢功能方面。冷冻保存后,EDT324中储存的胰岛的活力和刺激分别为92.4%和6.4,并且比慢速冷冻储存的胰岛(分别为72.5%和1.5)高。将链脲佐菌素诱导的糖尿病大鼠移植到冷冻保存在EDT324中的胰岛中,该胰岛可以纠正糖尿病并在移植后2天内实现血糖正常。这些结果表明,EDT324可成功冷冻保存大鼠胰岛以进行长期保存,作为传统使用的溶液(如10%DMSO)的替代解决方案。将冷冻保存的胰岛移植到糖尿病大鼠中可获得正常血糖。

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